HTG Molecular Diagnostics, Inc.
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About the company
HTG Molecular Diagnostics, Inc. operates as a life sciences company, specializing in the realm of precision medicine. They furnish specialized instruments, consumable products, and software applications engineered to automate the processing of samples and characterize a variety of molecular targets.
- CEO
- John L. Lubniewski
- IPO
- 2015
- Employees
- 53
- HQ
- Tucson, AZ, US
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- Market Cap
- $221
- P/E
- -0.00
- PEG
- -0.00
- P/S
- 0.00
- P/B
- 0.00
- EV/EBITDA
- 0.19
- Div Yield
- 0.00%
- Gross Margin
- 28.18%
- Op Margin
- -327.19%
- Net Margin
- -339.20%
- ROE
- -273.49%
- ROIC
- -151.00%
Latest fiscal year · YoY change
- Revenue
- $6.37M-28.5%
- Gross Profit
- $1.79M-62.7%
- Op Income
- $-20,829,596
- Net Income
- $-21,594,476-26.0%
- EPS
- $-24.28+18.1%
- OCF Growth
- -11.5%
- FCF Growth
- -7.5%
- 52W High
- $0.00
- 52W Low
- $0.00
- 50D MA
- $0.00
- 200D MA
- $0.00
- Beta
- 2.96
- RSI (14)
- 52
- Avg Volume
- 35
Earnings call summaries
Pick a quarter — each call distilled into takeaways, results, and a bull vs bear read.
HTG Molecular Diagnostics reported a softer second quarter as profiling revenue remained pressured by slow oncology trial activity, but management said HTP adoption, drug discovery milestones, and spending cuts are helping reposition the company for recovery.· August 11, 2022
- Q2 revenue was $1.5 million, down from $2.1 million a year ago, with the decline tied mainly to sluggish oncology market activity.
- HTP has become the company’s best-selling profiling product, with $0.6 million of transcriptome panel kits and VERI/O sample processing revenue in the quarter, over 40% of total revenue.
- Management said it hit all first-half development milestones in drug discovery, including an RNA modification assay and a second white paper supporting the platform.
- The company added 11 new customers, ended Q2 with 50 active pharma programs, and now has over 370 publications referencing HTG technology.
- HTG made “significant adjustments” to spending to contain cash burn and ended the quarter with $14.1 million in cash, cash equivalents and short-term available-for-sale securities.
Second-quarter 2022 revenue was $1.5 million versus $2.1 million in Q2 2021. Cost of product and product-related services revenue was $1.0 million, unchanged year over year, though Q2 2021 included about $160,000 of employee retention credits that did not recur in 2022. Research and development expense was $1.8 million versus $1.3 million a year ago; operating loss was $5.7 million versus $4.1 million; and net loss per share was $0.54 versus $0.39. Shaun McMeans said Q2 revenue was entirely direct revenue, and HTP-related transcriptome kits and VERI/O services totaled $0.6 million, over 40% of overall revenue. The company ended June 30, 2022 with $14.1 million in cash, cash equivalents and short-term available-for-sale securities. In July, HTG amended its senior credit facility to remove the minimum liquidity covenant and prepaid $2.5 million of principal without penalty; remaining payments continue monthly through the original maturity date of December 1, 2023. Management did not provide formal quarterly or full-year numeric guidance, but said it expects momentum in 2022 to continue, with more customer interest in HTP and additional drug discovery milestones ahead.
John Lubniewski framed the quarter as strategically important, saying HTG is evolving into a disruptive hybrid life science drug discovery company. He said the company achieved all of its first-half development milestones and that the drug discovery program is “on spec and on plan,” while also acknowledging profiling remains constrained by slower-than-expected recovery in oncology trials. His tone was optimistic but realistic, emphasizing new customer dialogues, broader disease-area opportunities, and the view that the next 12 months could be transformational.
Shaun McMeans focused on the financial pressure from lower revenue and on steps taken to preserve liquidity. He detailed the quarter’s $1.5 million revenue, $1.0 million cost of revenue, $1.8 million R&D expense, $5.7 million operating loss, and $14.1 million cash balance, and noted that 2021 comparisons were helped by employee retention credits that did not recur. He also highlighted the July credit facility amendment that removed the minimum liquidity covenant and allowed a $2.5 million principal prepayment without penalty, underscoring the company’s efforts to manage cash burn and strengthen the balance sheet.
Analysts asked about the first peer-reviewed HTP publication and how visible management is into future publications; John Lubniewski said the company has visibility and expects roughly 3 to 5 additional papers. He also said HTP and the microRNA product will likely make up the vast majority of profiling revenue going forward, with legacy panels used mainly to finish existing work. Another question addressed whether HTP is being used beyond oncology; management said yes, noting they are now getting in front of more customers and exploring broader disease areas and sample types that could open larger cohorts than oncology alone.
The positive case from the call is that HTP appears to be gaining traction quickly, becoming the company’s largest-selling product and drawing more interest from pharma customers. Management also sounded encouraged by multiple drug discovery milestones, the second white paper, and the prospect of more publications and customer programs in coming quarters.
The main risk remains that profiling revenue is still held back by a slow recovery in oncology trials, and management explicitly said the business has not returned to pre-pandemic levels. Revenue declined year over year, operating loss widened, and the company is still dependent on spending cuts and balance-sheet management while waiting for demand to improve.
AI summary of the company's earnings call · Paraphrased · Not investment advice
- Free Float
- 100.0%
- Shares Outstanding
- 2.21M
- Float Shares
- 2.21M
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